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Lacrimal Gland Repair Using Progenitor Cells
by
Dartt, Darlene A.
, Yoshida, Miya
, Makarenkova, Helen P.
, Gromova, Anastasia
, Voronov, Dmitry A.
, Meech, Robyn
, Thotakura, Suharika
in
Animals
/ Ataxin
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell adhesion molecules
/ Cell culture
/ Cell Differentiation
/ Cell lineage
/ Cell surface markers
/ Cell transplantation
/ Cellular therapy
/ Colony-Forming Units Assay
/ c‐kit
/ Data analysis
/ Disease
/ Epithelial Cell Adhesion Molecule - metabolism
/ Epithelial cells
/ Epithelial Cells - cytology
/ Fluorescence‐activated cell sorting
/ Gene expression
/ Growth factors
/ Inflammation
/ Lacrimal Apparatus - physiology
/ Lacrimal gland and Nasolacrimal duct
/ Mice, Inbred C57BL
/ Pluripotency
/ Progenitor cells
/ Proto-Oncogene Proteins c-kit - metabolism
/ Regeneration
/ Research centers
/ Runx1 protein
/ Stem Cell Transplantation
/ Stem cells
/ Stem Cells - cytology
/ Tears
/ Tissue‐Specific Progenitor and Stem Cells
/ Tissue‐specific stem cells
/ Transcription Factors - metabolism
/ Translational s and Reviews
2017
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Lacrimal Gland Repair Using Progenitor Cells
by
Dartt, Darlene A.
, Yoshida, Miya
, Makarenkova, Helen P.
, Gromova, Anastasia
, Voronov, Dmitry A.
, Meech, Robyn
, Thotakura, Suharika
in
Animals
/ Ataxin
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell adhesion molecules
/ Cell culture
/ Cell Differentiation
/ Cell lineage
/ Cell surface markers
/ Cell transplantation
/ Cellular therapy
/ Colony-Forming Units Assay
/ c‐kit
/ Data analysis
/ Disease
/ Epithelial Cell Adhesion Molecule - metabolism
/ Epithelial cells
/ Epithelial Cells - cytology
/ Fluorescence‐activated cell sorting
/ Gene expression
/ Growth factors
/ Inflammation
/ Lacrimal Apparatus - physiology
/ Lacrimal gland and Nasolacrimal duct
/ Mice, Inbred C57BL
/ Pluripotency
/ Progenitor cells
/ Proto-Oncogene Proteins c-kit - metabolism
/ Regeneration
/ Research centers
/ Runx1 protein
/ Stem Cell Transplantation
/ Stem cells
/ Stem Cells - cytology
/ Tears
/ Tissue‐Specific Progenitor and Stem Cells
/ Tissue‐specific stem cells
/ Transcription Factors - metabolism
/ Translational s and Reviews
2017
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Lacrimal Gland Repair Using Progenitor Cells
by
Dartt, Darlene A.
, Yoshida, Miya
, Makarenkova, Helen P.
, Gromova, Anastasia
, Voronov, Dmitry A.
, Meech, Robyn
, Thotakura, Suharika
in
Animals
/ Ataxin
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell adhesion molecules
/ Cell culture
/ Cell Differentiation
/ Cell lineage
/ Cell surface markers
/ Cell transplantation
/ Cellular therapy
/ Colony-Forming Units Assay
/ c‐kit
/ Data analysis
/ Disease
/ Epithelial Cell Adhesion Molecule - metabolism
/ Epithelial cells
/ Epithelial Cells - cytology
/ Fluorescence‐activated cell sorting
/ Gene expression
/ Growth factors
/ Inflammation
/ Lacrimal Apparatus - physiology
/ Lacrimal gland and Nasolacrimal duct
/ Mice, Inbred C57BL
/ Pluripotency
/ Progenitor cells
/ Proto-Oncogene Proteins c-kit - metabolism
/ Regeneration
/ Research centers
/ Runx1 protein
/ Stem Cell Transplantation
/ Stem cells
/ Stem Cells - cytology
/ Tears
/ Tissue‐Specific Progenitor and Stem Cells
/ Tissue‐specific stem cells
/ Transcription Factors - metabolism
/ Translational s and Reviews
2017
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Journal Article
Lacrimal Gland Repair Using Progenitor Cells
2017
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Overview
In humans, the lacrimal gland (LG) is the primary contributor to the aqueous layer of the tear film. Production of tears in insufficient quantity or of inadequate quality may lead to aqueous‐deficiency dry eye (ADDE). Currently there is no cure for ADDE. The development of strategies to reliably isolate LG stem/progenitor cells from the LG tissue brings great promise for the design of cell replacement therapies for patients with ADDE. We analyzed the therapeutic potential of epithelial progenitor cells (EPCPs) isolated from adult wild‐type mouse LGs by transplanting them into the LGs of TSP ‐1−/− mice, which represent a novel mouse model for ADDE. TSP‐1−/− mice are normal at birth but progressively develop a chronic form of ocular surface disease, characterized by deterioration, inflammation, and secretory dysfunction of the lacrimal gland. Our study shows that, among c‐kit‐positive epithelial cell adhesion molecule (EpCAM+) populations sorted from mouse LGs, the c‐kit+dim/EpCAM+/Sca1 − /CD34 − /CD45 − cells have the hallmarks of an epithelial cell progenitor population. Isolated EPCPs express pluripotency factors and markers of the epithelial cell lineage Runx1 and EpCAM, and they form acini and ducts when grown in reaggregated three‐dimensional cultures. Moreover, when transplanted into injured or “diseased” LGs, they engraft into acinar and ductal compartments. EPCP‐injected TSP‐1−/− LGs showed reduction of cell infiltration, differentiation of the donor EPCPs within secretory acini, and substantial improvement in LG structural integrity and function. This study provides the first evidence for the effective use of adult EPCP cell transplantation to rescue LG dysfunction in a model system. Stem Cells Translational Medicine 2017;6:88–98
Publisher
Oxford University Press,John Wiley and Sons Inc
Subject
/ Ataxin
/ c‐kit
/ Disease
/ Epithelial Cell Adhesion Molecule - metabolism
/ Fluorescence‐activated cell sorting
/ Lacrimal Apparatus - physiology
/ Lacrimal gland and Nasolacrimal duct
/ Proto-Oncogene Proteins c-kit - metabolism
/ Tears
/ Tissue‐Specific Progenitor and Stem Cells
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